NDUFA2 antibody (AA 1-95)

Catalog No. ABIN6144461

Product Details anti-NDUFA2 Antibody

Target: NDUFA2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 2, 8kDa (NDUFA2))

Binding Specificity: AA 1-95

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFA2 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Sequence: MAAAAASRGV GAKLGLREIR IHLCQRSPGS QGVRDFIEKR YVELKKANPD LPILIRECSD VQPKLWARYA FGQETNVPLN NFSADQVTRA LENVL

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-95 of human NDUFA2 (NP_002479.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:200

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for NDUFA2

Target: NDUFA2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 2, 8kDa (NDUFA2))

Alternative Name: NDUFA2 (NDUFA2 Products)

Synonyms: NDUFA2 antibody, b8 antibody, cd14 antibody, cib8 antibody, AV000592 antibody, B8 antibody, C1-B8 antibody, CI-B8 antibody, CD14 antibody, CIB8 antibody, NADH:ubiquinone oxidoreductase subunit A2 antibody, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 antibody, Ndufa2 antibody, NDUFA2 antibody, ndufa2 antibody

Background: The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.,NDUFA2,B8,CD14,CIB8,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFA2

Molecular Weight: 8 kDa/10 kDa

Gene ID: 4695

UniProt: O43678